Rusan Pharma: Over 30 years of specializing in the treatment of Addiction and Pain Management.
01 1M/s. Rusan Pharma Limited
01 1Eflornithine Hydrochloride Monohydrate IH
01 1WC-0278
01 1India
Rusan Pharma: Over 30 years of specializing in the treatment of Addiction and Pain Management.
Eflornithine Hydrochloride Monohydrate IH
Date of Issue : 2021-08-27
Valid Till : 2024-06-10
Written Confirmation Number : WC-0278
Address of the Firm : Plot No. 6406, GIDC Estate, Ankleshwar-393002, Dist. Bharuch, Gujarat
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A Ornithine, 2-(difluoromethyl)-, monohydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ornithine, 2-(difluoromethyl)-, monohydrochloride, including repackagers and relabelers. The FDA regulates Ornithine, 2-(difluoromethyl)-, monohydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ornithine, 2-(difluoromethyl)-, monohydrochloride API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Ornithine, 2-(difluoromethyl)-, monohydrochloride supplier is an individual or a company that provides Ornithine, 2-(difluoromethyl)-, monohydrochloride active pharmaceutical ingredient (API) or Ornithine, 2-(difluoromethyl)-, monohydrochloride finished formulations upon request. The Ornithine, 2-(difluoromethyl)-, monohydrochloride suppliers may include Ornithine, 2-(difluoromethyl)-, monohydrochloride API manufacturers, exporters, distributors and traders.
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A Ornithine, 2-(difluoromethyl)-, monohydrochloride written confirmation (Ornithine, 2-(difluoromethyl)-, monohydrochloride WC) is an official document issued by a regulatory agency to a Ornithine, 2-(difluoromethyl)-, monohydrochloride manufacturer, verifying that the manufacturing facility of a Ornithine, 2-(difluoromethyl)-, monohydrochloride active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Ornithine, 2-(difluoromethyl)-, monohydrochloride APIs or Ornithine, 2-(difluoromethyl)-, monohydrochloride finished pharmaceutical products to another nation, regulatory agencies frequently require a Ornithine, 2-(difluoromethyl)-, monohydrochloride WC (written confirmation) as part of the regulatory process.
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